Canonical Allele Identifier: CA414810525
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.11589T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11589T>G , J01415.2:m.11589T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.830T>G ENSP00000354961.2:p.Leu277Arg